{"title":"锌-三唑烷金属有机框架辅助合成掺氮碳中封装的锗纳米颗粒作为锂离子电池的负极材料","authors":"Zhuo Wang, Xue Bai, Jiabao Dong, Kexin Zhang, Bin Zhao, Xiaoli Dong","doi":"10.1002/batt.202400442","DOIUrl":null,"url":null,"abstract":"Germanium (Ge) is demonstrated to be prospective as a lithium‐ion battery anode material, yet the cycling stability is undermined by substantial volume fluctuations, restricting its viability for practical applications. Here, we present a facile Zn‐based metal−organic framework (MOF) engaged route to produce Ge nanoparticles in situ encapsulated in nitrogen‐doped mesoporous carbon (denoted as Ge@N‐C) as an anode material. This method uses a zinc‐triazolate MOF (MET‐6) and commercial GeO2 as the hybrid carbon and Ge precursors. After a heating treatment, the Ge@N‐C composite is readily obtained along with the simultaneous thermal decomposition of MET‐6 and the reduction of GeO2. Benefiting from the mesoporous structure and high electrical conductivity of N‐C, along with the strong interaction between Ge and N‐C, the obtained Ge@N‐C electrode exhibits a significant reversible charge capacity of 1012.8 mAh g‐1 after 150 cycles at 0.1 A g‐1, and excellent rate capability. Furthermore, a reversible charge capacity of 521.1 mAh g‐1 can be maintained at 5.0 A g‐1 after 1000 cycles.","PeriodicalId":132,"journal":{"name":"Batteries & Supercaps","volume":"309 1","pages":""},"PeriodicalIF":5.1000,"publicationDate":"2024-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Zinc‐Triazolate Metal‐Organic Framework Assisted Synthesis of Germanium Nanoparticles Encapsulated in Nitrogen‐Doped Carbon as Anode Materials for Lithium‐Ion Batteries\",\"authors\":\"Zhuo Wang, Xue Bai, Jiabao Dong, Kexin Zhang, Bin Zhao, Xiaoli Dong\",\"doi\":\"10.1002/batt.202400442\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Germanium (Ge) is demonstrated to be prospective as a lithium‐ion battery anode material, yet the cycling stability is undermined by substantial volume fluctuations, restricting its viability for practical applications. Here, we present a facile Zn‐based metal−organic framework (MOF) engaged route to produce Ge nanoparticles in situ encapsulated in nitrogen‐doped mesoporous carbon (denoted as Ge@N‐C) as an anode material. This method uses a zinc‐triazolate MOF (MET‐6) and commercial GeO2 as the hybrid carbon and Ge precursors. After a heating treatment, the Ge@N‐C composite is readily obtained along with the simultaneous thermal decomposition of MET‐6 and the reduction of GeO2. Benefiting from the mesoporous structure and high electrical conductivity of N‐C, along with the strong interaction between Ge and N‐C, the obtained Ge@N‐C electrode exhibits a significant reversible charge capacity of 1012.8 mAh g‐1 after 150 cycles at 0.1 A g‐1, and excellent rate capability. Furthermore, a reversible charge capacity of 521.1 mAh g‐1 can be maintained at 5.0 A g‐1 after 1000 cycles.\",\"PeriodicalId\":132,\"journal\":{\"name\":\"Batteries & Supercaps\",\"volume\":\"309 1\",\"pages\":\"\"},\"PeriodicalIF\":5.1000,\"publicationDate\":\"2024-09-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Batteries & Supercaps\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1002/batt.202400442\",\"RegionNum\":4,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ELECTROCHEMISTRY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Batteries & Supercaps","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/batt.202400442","RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0
摘要
锗(Ge)作为锂离子电池负极材料具有广阔的发展前景,但其循环稳定性因体积大幅波动而受到影响,限制了其在实际应用中的可行性。在此,我们提出了一种简便的锌基金属有机框架(MOF)参与路线,以原位生产封装在掺氮介孔碳(Ge@N-C)中的 Ge 纳米粒子,作为负极材料。该方法使用三唑锌MOF(MET-6)和商用GeO2作为碳和Ge的混合前驱体。加热处理后,随着 MET-6 的热分解和 GeO2 的还原,很容易得到 Ge@N-C 复合材料。得益于 N-C 的介孔结构和高导电性,以及 Ge 与 N-C 之间的强相互作用,所获得的 Ge@N-C 电极在 0.1 A g-1 的条件下循环 150 次后,显示出 1012.8 mAh g-1 的显著可逆电荷容量和优异的速率能力。此外,在 5.0 A g-1 条件下循环 1000 次后,可保持 521.1 mAh g-1 的可逆充电容量。
Zinc‐Triazolate Metal‐Organic Framework Assisted Synthesis of Germanium Nanoparticles Encapsulated in Nitrogen‐Doped Carbon as Anode Materials for Lithium‐Ion Batteries
Germanium (Ge) is demonstrated to be prospective as a lithium‐ion battery anode material, yet the cycling stability is undermined by substantial volume fluctuations, restricting its viability for practical applications. Here, we present a facile Zn‐based metal−organic framework (MOF) engaged route to produce Ge nanoparticles in situ encapsulated in nitrogen‐doped mesoporous carbon (denoted as Ge@N‐C) as an anode material. This method uses a zinc‐triazolate MOF (MET‐6) and commercial GeO2 as the hybrid carbon and Ge precursors. After a heating treatment, the Ge@N‐C composite is readily obtained along with the simultaneous thermal decomposition of MET‐6 and the reduction of GeO2. Benefiting from the mesoporous structure and high electrical conductivity of N‐C, along with the strong interaction between Ge and N‐C, the obtained Ge@N‐C electrode exhibits a significant reversible charge capacity of 1012.8 mAh g‐1 after 150 cycles at 0.1 A g‐1, and excellent rate capability. Furthermore, a reversible charge capacity of 521.1 mAh g‐1 can be maintained at 5.0 A g‐1 after 1000 cycles.
期刊介绍:
Electrochemical energy storage devices play a transformative role in our societies. They have allowed the emergence of portable electronics devices, have triggered the resurgence of electric transportation and constitute key components in smart power grids. Batteries & Supercaps publishes international high-impact experimental and theoretical research on the fundamentals and applications of electrochemical energy storage. We support the scientific community to advance energy efficiency and sustainability.